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Articles

Identification and characterization of lipoxygenase in fresh culinary herbs

, , &
Pages 1470-1478 | Received 23 Feb 2016, Accepted 07 Jul 2016, Published online: 14 Nov 2016

Figures & data

Table 1. Kinetic parameters (Vmax and KM) measured, at pH 6.0 and temperature of 37°C, for the oxidation of linoleic acid by LOX extracted from the three different culinary herbs. For each sample the protein content was also reported.

Figure 1 Specific activity (SA, U*mgCitation1protein*minCitation1), determined at pH 6.0 and temperature of 37°C, toward linoleic acid measured for the crude LOX extracted from basil (

), rosemary (
), and sage (
).

Figure 1 Specific activity (SA, U*mg−Citation1protein*min−Citation1), determined at pH 6.0 and temperature of 37°C, toward linoleic acid measured for the crude LOX extracted from basil (Display full size), rosemary (Display full size), and sage (Display full size).

Figure 2 Effect of pH on lipoxygenase activity extracted from basil (B,

), rosemary (R,
), and sage (S,
). Local optimum (100% relative activity, RA) was found at 37°C.

Figure 2 Effect of pH on lipoxygenase activity extracted from basil (B, Display full size), rosemary (R, Display full size), and sage (S, Display full size). Local optimum (100% relative activity, RA) was found at 37°C.

Figure 3 Effect of temperature on lipoxygenase extracted from basil (B,

), rosemary R,
), and sage (S,
).Local optimum (100% relative activity, RA) was found at pH 6.0.

Figure 3 Effect of temperature on lipoxygenase extracted from basil (B, Display full size), rosemary R, Display full size), and sage (S, Display full size).Local optimum (100% relative activity, RA) was found at pH 6.0.

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